Canonical Allele Identifier: CA6546878

Gene: KMT2D

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49039343C>T , CM000674.2:g.49039343C>T	GRCh38
NC_000012.11:g.49433126C>T , CM000674.1:g.49433126C>T	GRCh37
NC_000012.10:g.47719393C>T	NCBI36
NG_027827.1:g.20982G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003482.4:c.8245G>A MANE Select	NP_003473.3:p.Val2749Met
ENST00000301067.12:c.8245G>A MANE Select	ENSP00000301067.7:p.Val2749Met
NM_003482.3:c.8245G>A	NP_003473.3:p.Val2749Met
ENST00000301067.11:c.8245G>A	ENSP00000301067.7:p.Val2749Met
ENST00000683543.2:c.8245G>A	ENSP00000506726.1:p.Val2749Met
ENST00000685166.1:c.8254G>A	ENSP00000509386.1:p.Val2752Met
ENST00000689060.1:c.2264G>A
ENST00000689143.1:c.1918G>A	ENSP00000509839.1:p.Val640Met
ENST00000689944.1:c.2354G>A
ENST00000692637.1:c.8242G>A	ENSP00000509666.1:p.Val2748Met
XM_005269162.3:c.8245G>A	XP_005269219.1:p.Val2749Met
XM_005269162.4:c.8245G>A	XP_005269219.1:p.Val2749Met
XM_006719614.2:c.8254G>A	XP_006719677.1:p.Val2752Met
XM_006719614.4:c.8254G>A	XP_006719677.1:p.Val2752Met
XM_006719616.2:c.8242G>A	XP_006719679.1:p.Val2748Met
XM_006719616.3:c.8242G>A	XP_006719679.1:p.Val2748Met
XM_011538770.1:c.8254G>A	XP_011537072.1:p.Val2752Met
XM_011538770.2:c.8254G>A	XP_011537072.1:p.Val2752Met
XM_011538771.1:c.8251G>A	XP_011537073.1:p.Val2751Met
XM_011538771.2:c.8251G>A	XP_011537073.1:p.Val2751Met
XM_011538772.1:c.8245G>A	XP_011537074.1:p.Val2749Met
XM_011538772.2:c.8245G>A	XP_011537074.1:p.Val2749Met
XM_011538773.1:c.8242G>A	XP_011537075.1:p.Val2748Met
XM_011538773.2:c.8242G>A	XP_011537075.1:p.Val2748Met
XM_011538774.1:c.8233G>A	XP_011537076.1:p.Val2745Met
XM_011538774.2:c.8233G>A	XP_011537076.1:p.Val2745Met
XM_011538775.1:c.8254G>A	XP_011537077.1:p.Val2752Met
XM_011538776.1:c.8161G>A	XP_011537078.1:p.Val2721Met
XM_011538776.2:c.8161G>A	XP_011537078.1:p.Val2721Met
XR_001748874.1:n.9563G>A
XR_944740.1:n.10574G>A